Cargando…
Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing Radiation
Radiation biodosimeters are required urgently for fast and accurate evaluation of absorbed dose for irradiated individuals. Lipidomics has appeared as a credible technique for identification and quantification of lipid for researching biomarker of diseases. We performed a lipidomic profile on mice s...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180312/ https://www.ncbi.nlm.nih.gov/pubmed/32362795 http://dx.doi.org/10.1177/1559325820914209 |
_version_ | 1783525794548547584 |
---|---|
author | Huang, Jinfeng Wang, Qi Qi, Zhenhua Zhou, Shixiang Zhou, Meijuan Wang, Zhidong |
author_facet | Huang, Jinfeng Wang, Qi Qi, Zhenhua Zhou, Shixiang Zhou, Meijuan Wang, Zhidong |
author_sort | Huang, Jinfeng |
collection | PubMed |
description | Radiation biodosimeters are required urgently for fast and accurate evaluation of absorbed dose for irradiated individuals. Lipidomics has appeared as a credible technique for identification and quantification of lipid for researching biomarker of diseases. We performed a lipidomic profile on mice serum at time points of 6, 24, and 72 hours after 0, 2, 5.5, 7, and 8 Gy irradiation to select radiation-responsive lipids and conducted Kyoto Encyclopedia of Genes and Genome pathway enrichment analysis to recognize the pathways and network changes. Then, Pearson correlation analysis was performed to evaluate the feasibility of radiation-responsive lipids to estimate radiation dose. Seven radiation-responsive lipids including PC (18:2/18:2), PC (18:0/18:2), Lyso PC 18:1, PC (18:0/20:4), SM (D18:0/24:1), PC (16:0/18:1), and Lyso PC 18:2 were identified in which glycerophospholipid metabolism presented as the most significant pathway, and they all presented good linear correlation with the irradiated dose. This study identified 7 radiation-responsive lipids in mice serum and certificate their feasibility of dose estimation as biodosimeters. |
format | Online Article Text |
id | pubmed-7180312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-71803122020-05-01 Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing Radiation Huang, Jinfeng Wang, Qi Qi, Zhenhua Zhou, Shixiang Zhou, Meijuan Wang, Zhidong Dose Response Potential Biomarkers of Radiation Damage Radiation biodosimeters are required urgently for fast and accurate evaluation of absorbed dose for irradiated individuals. Lipidomics has appeared as a credible technique for identification and quantification of lipid for researching biomarker of diseases. We performed a lipidomic profile on mice serum at time points of 6, 24, and 72 hours after 0, 2, 5.5, 7, and 8 Gy irradiation to select radiation-responsive lipids and conducted Kyoto Encyclopedia of Genes and Genome pathway enrichment analysis to recognize the pathways and network changes. Then, Pearson correlation analysis was performed to evaluate the feasibility of radiation-responsive lipids to estimate radiation dose. Seven radiation-responsive lipids including PC (18:2/18:2), PC (18:0/18:2), Lyso PC 18:1, PC (18:0/20:4), SM (D18:0/24:1), PC (16:0/18:1), and Lyso PC 18:2 were identified in which glycerophospholipid metabolism presented as the most significant pathway, and they all presented good linear correlation with the irradiated dose. This study identified 7 radiation-responsive lipids in mice serum and certificate their feasibility of dose estimation as biodosimeters. SAGE Publications 2020-04-23 /pmc/articles/PMC7180312/ /pubmed/32362795 http://dx.doi.org/10.1177/1559325820914209 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Potential Biomarkers of Radiation Damage Huang, Jinfeng Wang, Qi Qi, Zhenhua Zhou, Shixiang Zhou, Meijuan Wang, Zhidong Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing Radiation |
title | Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing
Radiation |
title_full | Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing
Radiation |
title_fullStr | Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing
Radiation |
title_full_unstemmed | Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing
Radiation |
title_short | Lipidomic Profiling for Serum Biomarkers in Mice Exposed to Ionizing
Radiation |
title_sort | lipidomic profiling for serum biomarkers in mice exposed to ionizing
radiation |
topic | Potential Biomarkers of Radiation Damage |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180312/ https://www.ncbi.nlm.nih.gov/pubmed/32362795 http://dx.doi.org/10.1177/1559325820914209 |
work_keys_str_mv | AT huangjinfeng lipidomicprofilingforserumbiomarkersinmiceexposedtoionizingradiation AT wangqi lipidomicprofilingforserumbiomarkersinmiceexposedtoionizingradiation AT qizhenhua lipidomicprofilingforserumbiomarkersinmiceexposedtoionizingradiation AT zhoushixiang lipidomicprofilingforserumbiomarkersinmiceexposedtoionizingradiation AT zhoumeijuan lipidomicprofilingforserumbiomarkersinmiceexposedtoionizingradiation AT wangzhidong lipidomicprofilingforserumbiomarkersinmiceexposedtoionizingradiation |